Well-Defined Iron Sites in Crystalline Carbon Nitride

被引:20
作者
Genoux, Alexandre [1 ]
Pauly, Magnus [2 ]
Rooney, Conor L. [1 ]
Choi, Chungseok [1 ]
Shang, Bo [1 ]
McGuigan, Scott [2 ]
Fataftah, Majed S. [1 ]
Kayser, Yves [3 ]
Suhr, Simon C. B. [1 ]
Debeer, Serena [3 ]
Wang, Hailiang [1 ]
Maggard, Paul A. [2 ]
Holland, Patrick L. [1 ]
机构
[1] Yale Univ, Dept Chem, New Haven, CT 06520 USA
[2] North Carolina State Univ, Dept Chem, Raleigh, NC 27695 USA
[3] Max Planck Inst Chem Energy Convers, D-45470 Mulheim, Germany
关键词
ELECTRON-PARAMAGNETIC-RESONANCE; HIGH-SPIN; ELECTROCATALYTIC REDUCTION; MOSSBAUER-SPECTROSCOPY; DUAL-SITES; NITRATE; COMPLEXES; COORDINATION; NANOSHEETS; NANOTUBES;
D O I
10.1021/jacs.3c05417
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Carbon nitride materials can be hosts for transition metal sites, but Mo ssbauer studies on iron complexes in carbon nitrides have always shown a mixture of environments and oxidation states. Here we describe the synthesis and characterization of a crystalline carbon nitride with stoichiometric iron sites that all have the same environment. The material (formula C6N9H2Fe0.4Li1.2Cl, abbreviated PTI/FeCl2) is derived from reacting poly(triazine imide)center dot LiCl (PTI/LiCl) with a low-melting FeCl2/KCl flux, followed by anaerobic rinsing with methanol. X-ray diffraction, X-ray absorption and Mossbauer spectroscopies, and SQUID magnetometry indicate that there are tetrahedral high-spin iron(II) sites throughout the material, all having the same geometry. The material is active for electrocatalytic nitrate reduction to ammonia, with a production rate of ca. 0.1 mmol cm(-2) h(-1) and Faradaic efficiency of ca. 80% at -0.80 V vs RHE.
引用
收藏
页码:20739 / 20744
页数:6
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